dc.contributor.author | Akgul S.U. | |
dc.contributor.author | Cinar C.K. | |
dc.contributor.author | Caliskan Y. | |
dc.contributor.author | Demir E. | |
dc.contributor.author | Cebeci E. | |
dc.contributor.author | Meral R. | |
dc.contributor.author | Temurhan S. | |
dc.date.accessioned | 2024-02-04T13:30:04Z | |
dc.date.available | 2024-02-04T13:30:04Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 03011623 | |
dc.identifier.uri | https://doi.org/10.1007/s11255-022-03376-1 | |
dc.identifier.uri | http://hdl.handle.net/11446/4835 | |
dc.description.abstract | Purpose: The impact of core 1,3-galactosyltransferase-specific molecular chaperon (COSMC) gene expression and methylation profile on clinical progression of IgA nephropathy (IgAN) is unclear. The aim of this study was to determine the clinical significance and the relation of the COSMC gene expression and methylation pattern with the progression of IgAN. Methods: Thirty-nine biopsy-confirmed IgAN patients, 11 healthy relatives and 20 healthy controls were recruited. The COSMC mRNA levels and methylation profile of COSMC gene promoter were measured using the quantitative real-time PCR. The galactose-deficient IgA1 (Gd-IgA1) levels were measured using ELISA in serum and cell culture supernatant. The effect of IL-4 and AZA on COSMC expression and methylation and the correlation of COSMC gene expression and methylation levels with baseline kidney function tests, histology and long-term outcomes were examined. Results: The mean COSMC mRNA level was significantly lower, and serum Gd-IgA1 level was higher in IgAN patients compared with the control groups (p < 0.001, and p = < 0.001, respectively). The COSMC mRNA levels were correlated with intensity of hematuria (r = ? 0.41, p = 0.009), serum creatinine level (r = ? 0.37, p = 0.002) and eGFR (r = 0.36, p = 0.002). The COSMC methylation levels were correlated with age (r = 0.25, p = 0.04) and baseline eGFR (r = ? 0.326, p = 0.006). Twenty IgAN patients (51.3%) reached to complete (5, 12.8%) or partial remission (15, 38.5%) after a median of 34.5 months (IQR, 13.75–71). In multivariable Cox regression analysis, COSMC mRNA expression (adjusted HR (aHR) 1.871, 95% CI 1.287–2.722, p = 0.001) and Oxford T score (aHR 0.355, 95% CI 0.146–0.859, p = 0.022) predicted the remission. Conclusion: COSMC mRNA level is a novel biomarker candidate to predict the remission in IgAN patients. © 2022, The Author(s), under exclusive licence to Springer Nature B.V. | en_US |
dc.description.sponsorship | This Project was supported by the Istanbul University Scientific Research Unit (Project ID:55868). | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Springer Science and Business Media B.V. | en_US |
dc.relation.ispartof | International Urology and Nephrology | en_US |
dc.identifier.doi | 10.1007/s11255-022-03376-1 | |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Core 1,3-galactosyltransferase-specific molecular chaperone (COSMC) | en_US |
dc.subject | DNA methylation | en_US |
dc.subject | Galactose-deficient immunoglobulin A1 (Gd-IgA1) | en_US |
dc.subject | IgA nephropathy | en_US |
dc.subject | biological marker | en_US |
dc.subject | creatinine | en_US |
dc.subject | galactose | en_US |
dc.subject | immunoglobulin A1 | en_US |
dc.subject | immunoglobulin AN | en_US |
dc.subject | interleukin 4 | en_US |
dc.subject | messenger RNA | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | chaperone | en_US |
dc.subject | galactosyl-deficient IgA1 | en_US |
dc.subject | immunoglobulin A | en_US |
dc.subject | messenger RNA | en_US |
dc.subject | adult | en_US |
dc.subject | age | en_US |
dc.subject | Article | en_US |
dc.subject | B lymphocyte | en_US |
dc.subject | clinical article | en_US |
dc.subject | controlled study | en_US |
dc.subject | COSMC gene | en_US |
dc.subject | creatinine blood level | en_US |
dc.subject | disease association | en_US |
dc.subject | disease exacerbation | en_US |
dc.subject | DNA methylation | en_US |
dc.subject | enzyme linked immunosorbent assay | en_US |
dc.subject | estimated glomerular filtration rate | en_US |
dc.subject | female | en_US |
dc.subject | gene | en_US |
dc.subject | gene expression | en_US |
dc.subject | hematuria | en_US |
dc.subject | histopathology | en_US |
dc.subject | human | en_US |
dc.subject | human cell | en_US |
dc.subject | human tissue | en_US |
dc.subject | immunoglobulin A nephropathy | en_US |
dc.subject | immunoglobulin blood level | en_US |
dc.subject | kidney function test | en_US |
dc.subject | male | en_US |
dc.subject | outcome assessment | en_US |
dc.subject | promoter region | en_US |
dc.subject | real time polymerase chain reaction | en_US |
dc.subject | remission | en_US |
dc.subject | scoring system | en_US |
dc.subject | genetics | en_US |
dc.subject | immunoglobulin A nephropathy | en_US |
dc.subject | metabolism | en_US |
dc.subject | Glomerulonephritis, IGA | en_US |
dc.subject | Humans | en_US |
dc.subject | Immunoglobulin A | en_US |
dc.subject | Molecular Chaperones | en_US |
dc.subject | RNA, Messenger | en_US |
dc.title | COSMC expression as a predictor of remission in IgA nephropathy | en_US |
dc.type | article | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.volume | 55 | en_US |
dc.identifier.startpage | 1033 | en_US |
dc.identifier.endpage | 1044 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | Akgul, S.U., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey, Transplant Immunology Research Center of Excellence, Koç University, Istanbul, Turkey; Cinar, C.K., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Caliskan, Y., Division of Nephrology, Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, Capa/Fatih, Istanbul, Turkey, Division of Nephrology, Saint Louis University School of Medicine, Saint Louis, MO, United States; Demir, E., Division of Nephrology, Saint Louis University School of Medicine, Saint Louis, MO, United States; Cebeci, E., Department of Nephrology, Health Sciences University, Haseki Training and Research Hospital, Istanbul, Turkey; Meral, R., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Temurhan, S., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Ozluk, Y., Department of Pathology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey; Aydin, F., Department of Medical Biology and Genetics, Demiroglu Science University, Istanbul, Turkey; Oguz, F.S., Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey | en_US |
dc.identifier.pmid | 36306048 | en_US |
dc.identifier.scopus | 2-s2.0-85140874898 | en_US |
dc.authorscopusid | 55668931400 | |
dc.authorscopusid | 6504219013 | |
dc.authorscopusid | 55920704400 | |
dc.authorscopusid | 57192836887 | |
dc.authorscopusid | 37051798700 | |
dc.authorscopusid | 57193747679 | |
dc.authorscopusid | 26031760100 | |